MTLN mitoregulin
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | LEMP |
| SYNONYM | LINC00116 |
| SYNONYM | MOXI |
| SYNONYM | MPM |
| SYNONYM | NCRNA00116 |
| SYNONYM | SMIM37 |
| SYNONYM | TILR |
| MIM | 620770 OMIM |
| HGNC | HGNC:27339 HGNC |
| Ensembl | ENSG00000175701 Ensembl |
| AllianceGenome | HGNC:27339 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000611969.5 | hg38 | chr2 | 110,211,529 | 110,212,547 | 1,019 |
| ENST00000426713.1 | hg38 | chr2 | 110,211,530 | 110,212,823 | 1,294 |
| ENST00000414416.2 | hg38 | chr2 | 110,211,529 | 110,245,420 | 33,892 |
| ENST00000611969.5 | hg19 | chr2 | 110,969,106 | 110,970,124 | 1,019 |
| ENST00000414416.2 | hg19 | chr2 | 110,969,106 | 111,002,997 | 33,892 |
| ENST00000426713.1 | hg19 | chr2 | 110,969,107 | 110,970,400 | 1,294 |
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